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Making available information from studies sponsored by the pharmaceutical industry: some current practices
Authors:O'Kelly Michael  Julious Steven A  Pyke Stephen  Day Simon  Todd Sue  Seldrup Jorgen  Matcham James
Affiliation:Quintiles Ireland Ltd, Dublin, Ireland. mokelly@quintiles.com
Abstract:Since the web-based registry ClinicalTrials.gov was launched on 29 February 2000, the pharmaceutical industry has made available an increasing amount of information about the clinical trials that it sponsors. The process has been spurred on by a number of factors including a wish by the industry to provide greater transparency regarding clinical trial data; and has been both aided and complicated by the number of institutions that have a legitimate interest in guiding and defining what should be made available. This article reviews the history of this process of making information about clinical trials publicly available. It provides a reader's guide to the study registries and the databases of results; and looks at some indicators of consistency in the posting of study information.
Keywords:disclosure  clinical trials  publication bias  pharmaceutical industry  regulatory requirements  clinical trial registry
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